NDC 72789-509 – PredniSONE Tablets, USP, 20 mg
Prednisone 20 mg/1 · Tablet · Oral
Product NDC72789-509
Product details
- Brand name
- PredniSONE Tablets, USP, 20 mg
- Generic name
- PredniSONE
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA212629
- Marketed since
- May 22, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Corticosteroid
Active ingredients
- Prednisone 20 mg/1
Uses, dosage, side effects and warnings for PredniSONE Tablets, USP, 20 mg →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 72789-509-06 | 6 TABLET in 1 BOTTLE, PLASTIC (72789-509-06) | Jun 20, 2025 |
| 72789-509-09 | 9 TABLET in 1 BOTTLE, PLASTIC (72789-509-09) | May 27, 2025 |
| 72789-509-12 | 12 TABLET in 1 BOTTLE, PLASTIC (72789-509-12) | Jul 9, 2025 |
| 72789-509-15 | 15 TABLET in 1 BOTTLE, PLASTIC (72789-509-15) | May 22, 2025 |
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